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FDA 510(k)

Three Way Stop Cock

K-Number: K223499 · 2023-07-21

Decision Date2023-07-21
Product CodeFMG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Three Way Stop Cock is the device name listed in this FDA 510(k) record. The listed applicant is M/S Romsons International. It received FDA 510(k) clearance on 2023-07-21 under 510(k) number K223499. The device is classified under product code FMG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Three Way Stop Cock?

Three Way Stop Cock is a medical device that received FDA 510(k) clearance on 2023-07-21. The listed applicant is M/S Romsons International. The 510(k) number is K223499.

When did Three Way Stop Cock receive FDA 510(k) clearance?

Three Way Stop Cock received FDA 510(k) clearance on 2023-07-21, under 510(k) number K223499.

Who is the listed applicant for Three Way Stop Cock?

The FDA 510(k) record lists M/S Romsons International as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Three Way Stop Cock?

The FDA product code for Three Way Stop Cock is FMG.

Related Devices (Code: FMG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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